SU471357A1 - The method of obtaining 1,2-bis- (dimethylamino) -ethane - Google Patents

The method of obtaining 1,2-bis- (dimethylamino) -ethane

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Publication number
SU471357A1
SU471357A1 SU1883719A SU1883719A SU471357A1 SU 471357 A1 SU471357 A1 SU 471357A1 SU 1883719 A SU1883719 A SU 1883719A SU 1883719 A SU1883719 A SU 1883719A SU 471357 A1 SU471357 A1 SU 471357A1
Authority
SU
USSR - Soviet Union
Prior art keywords
ethane
bis
obtaining
dimethylamino
ethylenediamine
Prior art date
Application number
SU1883719A
Other languages
Russian (ru)
Inventor
Валентина Павловна Денисенко
Раиса Федоровна Стаднийчук
Михаил Александрович Бутлеровский
Евгений Николаевич Белоконь
Мария Ирмовна Кагановская
Людмила Ивановна Науменко
Original Assignee
Черновицкий Медицинский Институт
Киевский Химфармзавод Им.Ломоносова
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Черновицкий Медицинский Институт, Киевский Химфармзавод Им.Ломоносова filed Critical Черновицкий Медицинский Институт
Priority to SU1883719A priority Critical patent/SU471357A1/en
Application granted granted Critical
Publication of SU471357A1 publication Critical patent/SU471357A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

3434

содержанием основного вещества 99,97% (вы-альдегидом, отличающийс  тем, что, сthe content of the basic substance is 99.97% (you aldehyde, characterized in that, with

ход 79% от теории на этилендиамин).целью увеличени  выхода целевого продукта.move 79% of theory on ethylene diamine). The goal of increasing the yield of the target product.

Предмет изобретени реакцию алкилировани  провод т при соот1 . Способ получени  1,2-бис-(диметилами-5 те и формальдегиду в мол х 1 : 10 : 4.The subject matter of the invention is an alkylation reaction carried out at an appropriately. The method of obtaining 1,2-bis- (dimethyl-5 te and formaldehyde in mol x 1: 10: 4.

но)-этана восстановительным алкилированнем2. Способ по п. 1, о т л и ч а ю щ и и с   тем,but) -ethane is reductive alkylated 2. The method according to claim 1, about tl and h a y i and so,

этилендиамина муравьиной кислотой и форм-что алкилирование провод т при 100°С.ethylenediamine formic acid and form alkylation is carried out at 100 ° C.

471357 471357

нощении этилендиамина к муравьиной кислоethylenediamine to formic acid

SU1883719A 1973-02-16 1973-02-16 The method of obtaining 1,2-bis- (dimethylamino) -ethane SU471357A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1883719A SU471357A1 (en) 1973-02-16 1973-02-16 The method of obtaining 1,2-bis- (dimethylamino) -ethane

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1883719A SU471357A1 (en) 1973-02-16 1973-02-16 The method of obtaining 1,2-bis- (dimethylamino) -ethane

Publications (1)

Publication Number Publication Date
SU471357A1 true SU471357A1 (en) 1975-05-25

Family

ID=20542698

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1883719A SU471357A1 (en) 1973-02-16 1973-02-16 The method of obtaining 1,2-bis- (dimethylamino) -ethane

Country Status (1)

Country Link
SU (1) SU471357A1 (en)

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